CHARLES MICRO PROBE— 510(k) K812857

Substantially Equivalent

Mid Laboratories, Inc.

FDA 510(k) clearance K812857 for CHARLES MICRO PROBE, Substantially Equivalent on 1982-02-05. Applicant: Mid Laboratories, Inc..

Clearance details

Applicant: Mid Laboratories, Inc.
Product code: Code HQE
Advisory panel: Ophthalmic
Date received: 1981-10-13
Decision date: 1982-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HQE

product code HQE

Injury: 156
Malfunction: 565
Total: 721

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.